# Argus Medical Co., Inc.

- Location (FDA's records): Walnut, CA
- FDA decisions: 6 (1995–1995): 6 510(k) clearances
- Product codes: HRX (2), GCJ (2), HIH (1), EOB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K950255: Argus Hysteroscopy Instrument System (Aug 24, 1995)
- K951624: Argus Medical Company Laparoscopic Discectomy Instrument System (Jul 26, 1995)
- K950242: Argus Arthroscopy Instrument System (May 15, 1995)
- K950297: Argus Endoscopic Plastic Surgery Instrument System (Mar 3, 1995)
- K946011: Argus Sinus Endoscopy Instrument System (Feb 17, 1995)
- K950378: Argus Laparoscopy Instrument System (Feb 9, 1995)

Source page: https://510kreport.com/company/argus-medical